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Gene Review

apaH  -  diadenosine tetraphosphatase

Escherichia coli str. K-12 substr. MG1655

Synonyms: ECK0050, JW0048, cfcB
 
 
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Disease relevance of apaH

  • Escherichia coli strains with abnormally high concentrations of bis(5'-nucleosidyl)-tetraphosphates (Ap4N) were constructed by disrupting the apaH gene that encodes Ap4N-hydrolase [1].
  • The ygdP and apaH genes of Salmonella enterica serovar Typhimurium (S. Typhimurium) encode two unrelated dinucleoside polyphosphate (NpnN) hydrolases [2].
 

High impact information on apaH

  • An apaH mutation causes AppppA to accumulate and affects motility and catabolite repression in Escherichia coli [3].
  • The normal level of 3 microM adenylated NpnN (ApnN) was increased 1.5-, 3.5-, and 10-fold in the ygdP, apaH and double mutants, respectively [2].
  • The were not sensitive to kasugamycin, the apaH- apaG- ksgA- strain filamented and stopped growing in the presence of this antibiotic at 600 micrograms/ml [1].
  • The growth inhibition was abolished upon complementation with a plasmid carrying an intact apaH gene [1].
  • CfcA11 has a mutation in glySa which encodes the alpha-subunit of glycyl-tRNA synthetase, and cfcB1 has an IS2 insertion in apaH which encodes Ap4A hydrolase [4].
 

Biological context of apaH

  • Previously, Blanchin-Roland et al. showed that ksgA and apaH form a complex operon (Mol. Gen. Genet. 205:515-522, 1986) [5].
  • This promoter, active in vivo, can account for p1-independent expression of the two distal cistrons, apaG and apaH [6].
  • The DNA sequences of the diadenosine tetraphosphatase gene (apaH) and of the flanking regions were determined [6].
  • The other open reading frame was located counterclockwise to the apaH-like gene [7].
 

Anatomical context of apaH

  • Disruption of ygdP, apaH individually, and disruption of both genes together reduced intracellular invasion of human HEp-2 epithelial cells by S [2].

References

 
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